| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes. (Human Disease Ontology, DOID_0050331) |
| External Link | http://www.omim.org/entry/149730 |
| Similar Terms | |
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3 genes associated with the ladd syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
